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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JIMD Reports|March 4, 2015

Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.

American Journal of Human Genetics|February 11, 1999

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.

Frontiers in Molecular Neuroscience|November 3, 2017

Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.

Pageof 9

Search research articles

Showing results (81-90 of 83) with videos related to

Sort By:

Pageof 9

You have reached the last page of results.This site can display upto 83 results.

JIMD Reports|March 4, 2015

Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial MyopathyI M L W Körver-Keularts, M de Visser, H D Bakker, et al.

American Journal of Human Genetics|February 11, 1999

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, S Olpin, B J Poorthuis, et al.

Frontiers in Molecular Neuroscience|November 3, 2017

Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.

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